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3-Bromo-2,6-dimethylaniline, with the chemical formula C8H10BrN, is an organic compound derived from aniline. It features a benzene ring with a bromine atom and two methyl groups attached, giving it unique chemical properties. This pale yellow solid at room temperature is a versatile intermediate in various chemical syntheses and serves as a building block in organic chemistry, predominantly utilized in research and development labs.

53874-26-3

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53874-26-3 Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-2,6-dimethylaniline is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Dye Industry:
In the dye industry, 3-Bromo-2,6-dimethylaniline is utilized as an intermediate in the production of dyes. Its chemical properties enable the creation of a range of colorants used in various applications, including textiles, plastics, and printing inks.
Used in Organic Chemistry Research and Development:
3-Bromo-2,6-dimethylaniline is employed as a building block in organic chemistry for research and development purposes. Its reactivity and structural features make it a valuable compound for creating new organic compounds and exploring novel chemical reactions.
Safety Note:
Due to its potential health and safety hazards, 3-Bromo-2,6-dimethylaniline should be handled and stored with care in appropriate laboratory conditions to ensure the safety of personnel and the integrity of the compound.

Check Digit Verification of cas no

The CAS Registry Mumber 53874-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,7 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53874-26:
(7*5)+(6*3)+(5*8)+(4*7)+(3*4)+(2*2)+(1*6)=143
143 % 10 = 3
So 53874-26-3 is a valid CAS Registry Number.

53874-26-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-2,6-dimethyl-aniline

1.2 Other means of identification

Product number -
Other names 3-bromo-2,6-dimethylphenylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:53874-26-3 SDS

53874-26-3Relevant academic research and scientific papers

INHIBITING HUMAN INTEGRIN α4β7

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, (2021/04/23)

Disclosed are small molecule antagonists of human α4β7 integrin, and methods of using them to treat a number of diseases and conditions.

BENZOTHIAZOL COMPOUNDS AND METHODS USING THE SAME FOR TREATING NEURODEGENERATIVE DISORDERS

-

, (2019/04/18)

The present disclosure provides a compound of general Formula (I) having c-abl kinase inhibitory activity or pharmaceutically acceptable salt thereof, a pharmaceutical composition comprising the compound, and a method useful to treat or prevent neurodegenerative diseases using the compound.

From Naproxen Repurposing to Naproxen Analogues and Their Antiviral Activity against Influenza A Virus

Dilly, Sébastien,Fotso Fotso, Aurélien,Lejal, Nathalie,Zedda, Gloria,Chebbo, Mohamad,Rahman, Fryad,Companys, Simon,Bertrand, Hélène C.,Vidic, Jasmina,Noiray, Magali,Alessi, Marie-Christine,Tarus, Bogdan,Quideau, Stéphane,Riteau, Béatrice,Slama-Schwok, Anny

, p. 7202 - 7217 (2018/08/01)

The nucleoprotein (NP) of influenza A virus (IAV) required for IAV replication is a promising target for new antivirals. We previously identified by in silico screening naproxen being a dual inhibitor of NP and cyclooxygenase COX2, thus combining antivira

QUINAZOLINE COMPOUNDS

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, (2015/06/11)

The present invention relates to quinazoline compounds of formula I that function as inhibitors of RET (rearranged during transfection) kinase enzyme activity: (Formula (I)) wherein X, R1, R2, R3, R4, R5, R6 and R7 are each as defined herein. The present invention also relates to processes for the preparation of these compounds, to pharmaceutical compositions comprising them, and to their use in the treatment of proliferative disorders, such as cancer, as well as other diseases or conditions in which RET kinase activity is implicated.

An electroluminescent compound and an electroluminescent device comprising the same

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, (2016/10/08)

The present invention relates to an organic light emitting compound represented by chemical formula 1, and an organic electroluminescent device comprising the same. The organic light emitting compound according to the present invention increases PL quantu

THIOPHENE-2-CARBOXAMIDE DERIVATIVES AS MODULATORS OF CCR9 RECEPTOR

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Page/Page column 39, (2009/05/29)

Provided are compounds of Formula (I) or of Formula (II) that are modulators of CCR9 receptor activity, compositions containing the compounds and methods of use of the compounds and compositions. In certain embodiments, provided are methods for treating or amelioratin diseases associated with modulation of CCR9 receptor activity.

Phenylenediamine urotensin-II receptor antagonists and CCR-9 antagonists

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, (2008/06/13)

The present invention relates to urotensin II receptor antagonists, CCR-9 antagonists, pharmaceutical compositions containing them and their use.

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